Senior Clinical Project Manager Jobs in District of Columbia
Senior Clinical Project Manager jobs in District of Columbia are highly active, concentrated in federally adjacent healthcare, pharmaceutical research, and clinical trials organizations anchored by the region's dense presence of government contractors, research institutions, and advocacy-driven health nonprofits. The heaviest hiring is in Washington DC proper, with additional demand in nearby Bethesda and Silver Spring, where employers such as MAXIMUS, Booz Allen Hamilton, and Leidos Health maintain long-standing operations. The most in-demand specialties are regulatory affairs oversight, oncology trial management, and health IT-integrated study coordination. Find a role that fits below and apply directly.
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Showing 5 of 549+ Senior Clinical Project Manager jobs
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
- Regulatory responsibilities include the oversight and/or responsibility for the Intuitional Review Board (IRB) submissions and other related regulatory forms (e.g. scientific review) and adhering to the timelines of the study start-up process; developing informed consent documents and other documents as applicable; supporting the safety of clinical research participants; ensureing the appropriate delegation of study related tasks (i.e. Delegation of Authority).
- Explains the informed consent process and the study to the research participant (e.g. purpose duration risks/benefits) and obtains all required signatures; ensures the research participant has sufficient time and opportunity to ask the investigator medical questions; documents the informed consent process in the source document and provides the research participant with a copy of the informed consent.
- Develops an effective recruitment plan (e.g. central recruitment core); recruits research participants and discuss study protocol; educates research participants about protocol expectations and meets with research participants for each visit and maintains accessibility to discuss any questions or concerns regarding the study;
- Oversees the development of advertising materials; participates in teleconferences and/or meetings to review study progress and conduct.
- Data entry responsibilities include the completion and maintenance of case report forms and reviews data against the research participant's medical record for completeness and accuracy; addressing all queries clarifications and outstanding data queries and appropriately communicating with the sponsor and/or Contract Research Organization (CRO); completing and submitting case report forms on as close to a real time basis as possible.
- Ensures proper collection processing and shipment of biospecimens and pharmacokinetics as applicable (e.g. centrifuge freezing refrigeration) and maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens;
- Assists with maintaining equipment (e.g. calibration preventive maintenance); communicates with manager investigator and sponsor regarding abnormal laboratory values; maintains Internal Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials.
- Study conduct responsibilities include research participant interviews and assessments at study visits as required by protocol; assessing and ensuring research participant safety through study participation; maintaining close communication with investigator;
- Attending investigator meetings as appropriate and communicating relevant information to the research team; understanding and proficiently communicating all components of research documents such as protocol investigator brochure and research instructions.
- Receives and maintains test articles from sponsor and inventory test articles; works with research pharmacist as applicable; stores test article supplies according to Food and Drug Administration (FDA) regulations and sponsor requirements; administers test article as appropriate;
- Retrieves test articles and calculates research participant compliance; maintains randomization and emergency codes of test article; documents on accountability log and research participant record (e.g. test article received used disposed).
- Ensures that non-serious and serious adverse events are properly identified documented and reported according to all applicable requirements; presents investigator with relevant information for determination of seriousness causality and intervention; acts on investigator's recommendation for adverse event intervention (e.g. stop test article call research participant re-test treat); maintains follow-up to determine resolution of adverse event.
- Understands and complies with rules for billing Medicare Medicaid and third party payors for services drugs devices tests and procedures rendered in the clinical research context;
- Responsible for reviewing understanding and accepting the billing matrix/billing plan generated by administration for research participants enrolled in clinical studies; ensures research participant stipends have been routed in a timely manner as applicable.
- Study close-out responsibilities include return or disposition of unused supplies per sponsors requirement; reconciling test article accountability; document research participants who are lost to follow-up or who have dropped out (e.g. causes contact efforts); ensuring long term storage of documents; submitting IRB closing report (i.e. termination) after sponsor has closed study site.
- Acts as a liaison with research participants investigators sponsors and healthcare professionals; prepares for site qualification study initiation monitoring and close-out visits;
- Ensures all research participant encounters are updated as appropriate and within one business day in clinical trial management system (CTMS); works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers.
Education
- Bachelor's degree or an allied health or related professional degree required, or equivalent work experience
- 2 years of relevant clinical research experience required
- Experience in a healthcare setting preferred
- Undergraduate and/or work experiences that demonstrates aptitude for research facilitation preferred
- Verbal and written communication skills.
- Basic computer skills preferred.
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
- Regulatory responsibilities include the oversight and/or responsibility for the Intuitional Review Board (IRB) submissions and other related regulatory forms (e.g. scientific review) and adhering to the timelines of the study start-up process; developing informed consent documents and other documents as applicable; supporting the safety of clinical research participants; ensureing the appropriate delegation of study related tasks (i.e. Delegation of Authority).
- Explains the informed consent process and the study to the research participant (e.g. purpose duration risks/benefits) and obtains all required signatures; ensures the research participant has sufficient time and opportunity to ask the investigator medical questions; documents the informed consent process in the source document and provides the research participant with a copy of the informed consent.
- Develops an effective recruitment plan (e.g. central recruitment core); recruits research participants and discuss study protocol; educates research participants about protocol expectations and meets with research participants for each visit and maintains accessibility to discuss any questions or concerns regarding the study;
- Oversees the development of advertising materials; participates in teleconferences and/or meetings to review study progress and conduct.
- Data entry responsibilities include the completion and maintenance of case report forms and reviews data against the research participant's medical record for completeness and accuracy; addressing all queries clarifications and outstanding data queries and appropriately communicating with the sponsor and/or Contract Research Organization (CRO); completing and submitting case report forms on as close to a real time basis as possible.
- Ensures proper collection processing and shipment of biospecimens and pharmacokinetics as applicable (e.g. centrifuge freezing refrigeration) and maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens;
- Assists with maintaining equipment (e.g. calibration preventive maintenance); communicates with manager investigator and sponsor regarding abnormal laboratory values; maintains Internal Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials.
- Study conduct responsibilities include research participant interviews and assessments at study visits as required by protocol; assessing and ensuring research participant safety through study participation; maintaining close communication with investigator;
- Attending investigator meetings as appropriate and communicating relevant information to the research team; understanding and proficiently communicating all components of research documents such as protocol investigator brochure and research instructions.
- Receives and maintains test articles from sponsor and inventory test articles; works with research pharmacist as applicable; stores test article supplies according to Food and Drug Administration (FDA) regulations and sponsor requirements; administers test article as appropriate;
- Retrieves test articles and calculates research participant compliance; maintains randomization and emergency codes of test article; documents on accountability log and research participant record (e.g. test article received used disposed).
- Ensures that non-serious and serious adverse events are properly identified documented and reported according to all applicable requirements; presents investigator with relevant information for determination of seriousness causality and intervention; acts on investigator's recommendation for adverse event intervention (e.g. stop test article call research participant re-test treat); maintains follow-up to determine resolution of adverse event.
- Understands and complies with rules for billing Medicare Medicaid and third party payors for services drugs devices tests and procedures rendered in the clinical research context;
- Responsible for reviewing understanding and accepting the billing matrix/billing plan generated by administration for research participants enrolled in clinical studies; ensures research participant stipends have been routed in a timely manner as applicable.
- Study close-out responsibilities include return or disposition of unused supplies per sponsors requirement; reconciling test article accountability; document research participants who are lost to follow-up or who have dropped out (e.g. causes contact efforts); ensuring long term storage of documents; submitting IRB closing report (i.e. termination) after sponsor has closed study site.
- Acts as a liaison with research participants investigators sponsors and healthcare professionals; prepares for site qualification study initiation monitoring and close-out visits;
- Ensures all research participant encounters are updated as appropriate and within one business day in clinical trial management system (CTMS); works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers.
Education
- Bachelor's degree or an allied health or related professional degree required, or equivalent work experience
- 2 years of relevant clinical research experience required
- Experience in a healthcare setting preferred
- Undergraduate and/or work experiences that demonstrates aptitude for research facilitation preferred
- Verbal and written communication skills.
- Basic computer skills preferred.
See All 549+ Senior Clinical Project Manager Jobs in District of Columbia
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Find JobsSenior Clinical Project Manager Jobs by City in District of Columbia
Where District of Columbia roles are concentrated, by current openings.
Senior Clinical Project Manager Job Market in District of Columbia
A snapshot from current District of Columbia openings, updated as new roles post.
Who's Hiring
- Children's National Hospital38
- Metrostar Systems22
- MedStar Health21
- Unity Health Care20
- Howard University Hospital13
Top Industries Hiring
- Healthcare & Medical Services68
- Technology & Software38
- Education30
- Consulting & Professional Services18
- Biotechnology & Pharmaceuticals9
What District of Columbia Employers Look For
The qualifications that appear most often in senior clinical project manager jobs across District of Columbia.
- Bachelor's or master's degree in life sciences, public health, or a related clinical field
- PMP, CAPM, or RAC certification recognized by District of Columbia clinical employers
- Five or more years managing Phase II through IV clinical trials end to end
- Direct experience with FDA regulatory submissions and GCP compliance requirements
- Proficiency in clinical trial management systems such as Medidata Rave or Veeva Vault
- Strong background coordinating cross-functional teams across CROs and sponsor organizations
Senior Clinical Project Manager Jobs in District of Columbia: Frequently Asked Questions
How do you become a senior clinical project manager in District of Columbia?
The path typically starts with a bachelor's degree in a life science, nursing, public health, or a related field, followed by several years in clinical research coordinator or project coordinator roles. District of Columbia does not require a state-issued license specific to clinical project management, but employers strongly favor the Project Management Professional credential or the Regulatory Affairs Certification from RAPS, both widely recognized across the region's government contractor and research institution landscape.
How much do senior clinical project managers make in District of Columbia?
Senior clinical project managers in District of Columbia earn a median of about $104,900 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $64,080 for the lowest 10% to over $194,170 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior clinical project managers in District of Columbia?
Employers hiring senior clinical project managers in District of Columbia right now include Children's National Hospital, Metrostar Systems, and MedStar Health, based on current listings on Migrate Mate as of July 2026. The District of Columbia market is especially active among federal health contractors and consulting firms with long-term government agency relationships.
Which District of Columbia cities have the most senior clinical project manager jobs?
The cities with the most senior clinical project manager openings in District of Columbia are Washington and Pentagon. Washington DC drives the largest share due to its concentration of federal agencies, health policy organizations, and government contractors, while Bethesda and Silver Spring attract demand from the National Institutes of Health campus and the pharmaceutical and biotech firms clustered in the Maryland suburbs.
Are there remote senior clinical project manager jobs in District of Columbia?
Yes, and more than many clinical roles allow, since senior project managers often work at the coordination and oversight level rather than directly on-site at clinical facilities. About 57% of senior clinical project manager openings tied to District of Columbia are remote or hybrid as of July 2026. Protocol management, vendor oversight, and regulatory document coordination are the functions most commonly performed remotely.
How can I get hired as a senior clinical project manager in District of Columbia with little or no experience?
The most realistic entry path is a clinical research coordinator role, which large District of Columbia area employers such as government contractors, NIH-affiliated research centers, and federally funded health nonprofits regularly hire for without requiring prior management experience. From there, candidates move into project lead or associate project manager positions. Earning a Clinical Research Associate certification through ACRP or SOCRA while in a coordinator role gives applicants a concrete credential edge with District of Columbia hiring managers.
Where can I find and apply to senior clinical project manager jobs in District of Columbia?
You can find and apply to senior clinical project manager jobs in District of Columbia on Migrate Mate, which lists current openings across the region. Search the available roles, find the ones that fit your background and goals, and apply directly to the employers posting them.
See All 549+ Senior Clinical Project Manager Jobs in District of Columbia
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